Canonical Allele Identifier: CA1590738592

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149980971A= , CM000667.2:g.149980971A=	GRCh38
NC_000005.9:g.149360534A= , CM000667.1:g.149360534A=	GRCh37
NC_000005.8:g.149340727A=	NCBI36
NG_007147.2:g.22089A= , LRG_684:g.22089A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286298.5:c.1378A= MANE Select	ENSP00000286298.4:p.Thr460=
ENST00000286298.4:c.1378A=	ENSP00000286298.4:p.Thr460=
ENST00000503336.1:c.372+2620A=	ENSP00000426053.1:n.372+2620A=
NM_000112.3:c.1378A= , LRG_684t1:c.1378A=	NP_000103.2:p.Thr460=
XM_017009191.2:c.1378A=	XP_016864680.1:p.Thr460=
NM_000112.4:c.1378A= MANE Select	NP_000103.2:p.Thr460=